Canonical Allele Identifier: CA2639263588

Gene: ACE

Linked Data

• gnomAD v4: 17-63488507-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488507C>A , CM000679.2:g.63488507C>A	GRCh38
NC_000017.10:g.61565868C>A , CM000679.1:g.61565868C>A	GRCh37
NC_000017.9:g.58919600C>A	NCBI36
NG_011648.1:g.16435C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2306-141C>A MANE Select	ENSP00000290866.4:n.2306-141C>A
ENST00000290863.10:c.584-141C>A	ENSP00000290863.6:n.584-141C>A
ENST00000290866.9:c.2306-141C>A	ENSP00000290866.4:n.2306-141C>A
ENST00000413513.7:c.584-141C>A	ENSP00000392247.3:n.584-141C>A
ENST00000428043.5:c.2306-141C>A	ENSP00000397593.2:n.2306-141C>A
ENST00000577647.2:c.584-141C>A	ENSP00000464149.1:n.584-141C>A
ENST00000578839.5:c.*376-141C>A	ENSP00000462110.2:n.*376-141C>A
ENST00000579204.1:c.487-63C>A	ENSP00000464629.1:n.487-63C>A
ENST00000579314.5:c.584-63C>A	ENSP00000462599.1:n.584-63C>A
ENST00000582005.5:c.*226-141C>A	ENSP00000462002.1:n.*226-141C>A
ENST00000582761.1:c.74-141C>A	ENSP00000462909.1:n.74-141C>A
ENST00000584865.5:n.252-141C>A
NM_000789.3:c.2306-141C>A	NP_000780.1:n.2306-141C>A
NM_001178057.1:c.584-141C>A	NP_001171528.1:n.584-141C>A
NM_152830.2:c.584-141C>A	NP_690043.1:n.584-141C>A
XM_005257110.1:c.1757-141C>A	XP_005257167.1:n.1757-141C>A
XM_006721737.2:c.644-141C>A	XP_006721800.2:n.644-141C>A
XM_006721737.3:c.644-141C>A	XP_006721800.2:n.644-141C>A
NM_000789.4:c.2306-141C>A MANE Select	NP_000780.1:n.2306-141C>A
NM_001178057.2:c.584-141C>A	NP_001171528.1:n.584-141C>A
NM_152830.3:c.584-141C>A	NP_690043.1:n.584-141C>A
NM_001382700.1:c.1739-141C>A	NP_001369629.1:n.1739-141C>A
NM_001382701.1:c.1454-141C>A	NP_001369630.1:n.1454-141C>A
NM_001382702.1:c.236-141C>A	NP_001369631.1:n.236-141C>A
NR_168483.1:n.606-63C>A